224 related articles for article (PubMed ID: 36153334)
1. Quantitative trait locus analysis for endophenotypes reveals genetic substrates of core symptom domains and neurocognitive function in autism spectrum disorder.
Lee IH; Koelliker E; Kong SW
Transl Psychiatry; 2022 Sep; 12(1):407. PubMed ID: 36153334
[TBL] [Abstract][Full Text] [Related]
2. Endophenotype trait domains for advancing gene discovery in autism spectrum disorder.
Mosconi MW; Stevens CJ; Unruh KE; Shafer R; Elison JT
J Neurodev Disord; 2023 Nov; 15(1):41. PubMed ID: 37993779
[TBL] [Abstract][Full Text] [Related]
3. Association between Neuroligin-1 polymorphism and plasma glutamine levels in individuals with autism spectrum disorder.
Lee IH; Walker DI; Lin Y; Smith MR; Mandl KD; Jones DP; Kong SW
EBioMedicine; 2023 Sep; 95():104746. PubMed ID: 37544204
[TBL] [Abstract][Full Text] [Related]
4. Evidence for contribution of common genetic variants within chromosome 8p21.2-8p21.1 to restricted and repetitive behaviors in autism spectrum disorders.
Tao Y; Gao H; Ackerman B; Guo W; Saffen D; Shugart YY
BMC Genomics; 2016 Mar; 17():163. PubMed ID: 26931105
[TBL] [Abstract][Full Text] [Related]
5. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
Chen R; Davis LK; Guter S; Wei Q; Jacob S; Potter MH; Cox NJ; Cook EH; Sutcliffe JS; Li B
Mol Autism; 2017; 8():14. PubMed ID: 28344757
[TBL] [Abstract][Full Text] [Related]
6. ASD Phenotype-Genotype Associations in Concordant and Discordant Monozygotic and Dizygotic Twins Stratified by Severity of Autistic Traits.
Hu VW; Devlin CA; Debski JJ
Int J Mol Sci; 2019 Aug; 20(15):. PubMed ID: 31382655
[TBL] [Abstract][Full Text] [Related]
7. High dimensional endophenotype ranking in the search for major depression risk genes.
Glahn DC; Curran JE; Winkler AM; Carless MA; Kent JW; Charlesworth JC; Johnson MP; Göring HH; Cole SA; Dyer TD; Moses EK; Olvera RL; Kochunov P; Duggirala R; Fox PT; Almasy L; Blangero J
Biol Psychiatry; 2012 Jan; 71(1):6-14. PubMed ID: 21982424
[TBL] [Abstract][Full Text] [Related]
8. Social responsiveness, an autism endophenotype: genomewide significant linkage to two regions on chromosome 8.
Lowe JK; Werling DM; Constantino JN; Cantor RM; Geschwind DH
Am J Psychiatry; 2015 Mar; 172(3):266-75. PubMed ID: 25727539
[TBL] [Abstract][Full Text] [Related]
9. Assessment of Neuroanatomical Endophenotypes of Autism Spectrum Disorder and Association With Characteristics of Individuals With Schizophrenia and the General Population.
Hwang G; Wen J; Sotardi S; Brodkin ES; Chand GB; Dwyer DB; Erus G; Doshi J; Singhal P; Srinivasan D; Varol E; Sotiras A; Dazzan P; Kahn RS; Schnack HG; Zanetti MV; Meisenzahl E; Busatto GF; Crespo-Facorro B; Pantelis C; Wood SJ; Zhuo C; Shinohara RT; Shou H; Fan Y; Di Martino A; Koutsouleris N; Gur RE; Gur RC; Satterthwaite TD; Wolf DH; Davatzikos C
JAMA Psychiatry; 2023 May; 80(5):498-507. PubMed ID: 37017948
[TBL] [Abstract][Full Text] [Related]
10. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium
Mol Autism; 2017; 8():21. PubMed ID: 28540026
[TBL] [Abstract][Full Text] [Related]
11. Endophenotypes: A conceptual link between anorexia nervosa and autism spectrum disorder.
Zhou ZC; McAdam DB; Donnelly DR
Res Dev Disabil; 2018 Nov; 82():153-165. PubMed ID: 29239739
[TBL] [Abstract][Full Text] [Related]
12. Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism.
Matoba N; Liang D; Sun H; Aygün N; McAfee JC; Davis JE; Raffield LM; Qian H; Piven J; Li Y; Kosuri S; Won H; Stein JL
Transl Psychiatry; 2020 Aug; 10(1):265. PubMed ID: 32747698
[TBL] [Abstract][Full Text] [Related]
13. ASD restricted and repetitive behaviors associated at 17q21.33: genes prioritized by expression in fetal brains.
Cantor RM; Navarro L; Won H; Walker RL; Lowe JK; Geschwind DH
Mol Psychiatry; 2018 Apr; 23(4):993-1000. PubMed ID: 28533516
[TBL] [Abstract][Full Text] [Related]
14. Look duration at the face as a developmental endophenotype: elucidating pathways to autism and ADHD.
Gui A; Mason L; Gliga T; Hendry A; Begum Ali J; Pasco G; Shephard E; Curtis C; Charman T; Johnson MH; Meaburn E; Jones EJH;
Dev Psychopathol; 2020 Oct; 32(4):1303-1322. PubMed ID: 33012299
[TBL] [Abstract][Full Text] [Related]
15. Infant social attention: an endophenotype of ASD-related traits?
Jones EJ; Venema K; Earl RK; Lowy R; Webb SJ
J Child Psychol Psychiatry; 2017 Mar; 58(3):270-281. PubMed ID: 27861851
[TBL] [Abstract][Full Text] [Related]
16. Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk.
Nudel R; Christiani CAJ; Ohland J; Uddin MJ; Hemager N; Ellersgaard DV; Spang KS; Burton BK; Greve AN; Gantriis DL; Bybjerg-Grauholm J; Jepsen JRM; Thorup AAE; Mors O; Nordentoft M; Werge T
Autism Res; 2020 Mar; 13(3):369-381. PubMed ID: 31577390
[TBL] [Abstract][Full Text] [Related]
17. Executive functioning and local-global visual processing: candidate endophenotypes for autism spectrum disorder?
Van Eylen L; Boets B; Cosemans N; Peeters H; Steyaert J; Wagemans J; Noens I
J Child Psychol Psychiatry; 2017 Mar; 58(3):258-269. PubMed ID: 27804132
[TBL] [Abstract][Full Text] [Related]
18. Childhood Academic Performance: A Potential Marker of Genetic Liability to Autism.
Guilfoyle J; Winston M; Sideris J; Martin GE; Nayar K; Bush L; Wassink T; Losh M
J Autism Dev Disord; 2023 May; 53(5):1989-2005. PubMed ID: 35194728
[TBL] [Abstract][Full Text] [Related]
19. Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.
Callaghan DB; Rogic S; Tan PPC; Calli K; Qiao Y; Baldwin R; Jacobson M; Belmadani M; Holmes N; Yu C; Li Y; Li Y; Kurtzke FE; Kuzeljevic B; Yu AY; Hudson M; Mcaughton AJM; Xu Y; Dionne-Laporte A; Girard S; Liang P; Separovic ER; Liu X; Rouleau G; Pavlidis P; Lewis MES
Clin Genet; 2019 Sep; 96(3):199-206. PubMed ID: 31038196
[TBL] [Abstract][Full Text] [Related]
20. A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?
Chaste P; Klei L; Sanders SJ; Hus V; Murtha MT; Lowe JK; Willsey AJ; Moreno-De-Luca D; Yu TW; Fombonne E; Geschwind D; Grice DE; Ledbetter DH; Mane SM; Martin DM; Morrow EM; Walsh CA; Sutcliffe JS; Lese Martin C; Beaudet AL; Lord C; State MW; Cook EH; Devlin B
Biol Psychiatry; 2015 May; 77(9):775-84. PubMed ID: 25534755
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
